Canonical Allele Identifier: CA1752441788

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150974993A= , CM000669.2:g.150974993A=	GRCh38
NC_000007.13:g.150672081A= , CM000669.1:g.150672081A=	GRCh37
NC_000007.12:g.150303014A=	NCBI36
NG_008916.1:g.7934T= , LRG_288:g.7934T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262186.10:c.77-52T= MANE Select	ENSP00000262186.5:n.77-52T=
ENST00000262186.9:c.77-52T=	ENSP00000262186.5:n.77-52T=
ENST00000430723.4:c.-101-52T=	ENSP00000387657.4:n.-101-52T=
ENST00000532957.5:n.300-52T=
NM_000238.3:c.77-52T= , LRG_288t1:c.77-52T=	NP_000229.1:n.77-52T=
NM_172056.2:c.77-52T= , LRG_288t2:c.77-52T=	NP_742053.1:n.77-52T=
XM_011516186.1:c.77-52T=	XP_011514488.1:n.77-52T=
XM_011516186.3:c.77-52T=	XP_011514488.1:n.77-52T=
XM_017012196.1:c.-102+32T=	XP_016867685.1:n.-102+32T=
NM_000238.4:c.77-52T= MANE Select	NP_000229.1:n.77-52T=